Decay accelerating factor regulates complement activation on glomerular epithelial cells.

RJ Quigg, A Nicholson-Weller, AV Cybulsky… - … (Baltimore, Md.: 1950 …, 1989 - journals.aai.org
RJ Quigg, A Nicholson-Weller, AV Cybulsky, J Badalamenti, DJ Salant
Journal of immunology (Baltimore, Md.: 1950), 1989journals.aai.org
Epithelial cells of the glomerular capillary are the site of C5b-9 mediated injury in rat
membranous nephropathy. We investigated the regulation of C activation by cultured
glomerular epithelial cells (GEC). Rat and human GEC were more resistant to C injury by
homologous C than heterologous C. In human GEC homologous C cytotoxicity was
enhanced by antiserum to decay accelerating factor (DAF) indicating that homologous C
activation was, at least in part, restricted by membrane DAF. Anti-DAF immunoprecipitated a …
Abstract
Epithelial cells of the glomerular capillary are the site of C5b-9 mediated injury in rat membranous nephropathy. We investigated the regulation of C activation by cultured glomerular epithelial cells (GEC). Rat and human GEC were more resistant to C injury by homologous C than heterologous C. In human GEC homologous C cytotoxicity was enhanced by antiserum to decay accelerating factor (DAF) indicating that homologous C activation was, at least in part, restricted by membrane DAF. Anti-DAF immunoprecipitated a 67-kDa protein from human glomeruli. In rat GEC, pronase and phosphatidylinositol-specific phospholipase C (which are known to inactivate human DAF) enhanced cytotoxicity by homologous C. Thus, DAF is present on human GEC in culture and in human kidney glomeruli, and a DAF-like protein is present on cultured rat GEC. These proteins regulate C activation in vitro and may play a role in controlling C activation on GEC in vivo.
journals.aai.org